JPS6036190A - 光記録媒体 - Google Patents

光記録媒体

Info

Publication number: JPS6036190A
Authority: JP; Japan
Prior art keywords: ring; group; resin; general formula; optical recording
Prior art date: 1983-08-09
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Granted

Application number

JP58145294A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0441066B2 (fr

Inventor

Noriyoshi Nanba

憲良南波

Shigeru Asami

浅見　茂

Toshiki Aoi

利樹青井

Kazuo Takahashi

一夫高橋

Akihiko Kuroiwa

黒岩　顕彦

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

TDK Corp

Original Assignee

TDK Corp

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1983-08-09

Filing date

1983-08-09

Publication date

1985-02-25

1983-08-09 Application filed by TDK Corp filed Critical TDK Corp

1983-08-09 Priority to JP58145294A priority Critical patent/JPS6036190A/ja

1985-02-25 Publication of JPS6036190A publication Critical patent/JPS6036190A/ja

1992-07-07 Publication of JPH0441066B2 publication Critical patent/JPH0441066B2/ja

Status Granted legal-status Critical Current

Links

230000003287 optical effect Effects 0.000 title claims abstract description 17
229920005989 resin Polymers 0.000 claims abstract description 29
239000011347 resin Substances 0.000 claims abstract description 29
125000003118 aryl group Chemical group 0.000 claims abstract description 18
ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims abstract description 14
150000001875 compounds Chemical class 0.000 claims abstract description 8
125000001041 indolyl group Chemical group 0.000 claims abstract description 6
FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims abstract description 3
229920000642 polymer Polymers 0.000 claims description 13
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
239000000758 substrate Substances 0.000 claims description 10
125000005647 linker group Chemical group 0.000 claims description 4
125000002883 imidazolyl group Chemical group 0.000 claims description 3
ODIRBFFBCSTPTO-UHFFFAOYSA-N 1,3-selenazole Chemical group C1=C[se]C=N1 ODIRBFFBCSTPTO-UHFFFAOYSA-N 0.000 claims description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 2
150000001450 anions Chemical class 0.000 claims description 2
239000000178 monomer Substances 0.000 claims 1
125000002971 oxazolyl group Chemical group 0.000 claims 1
239000000975 dye Substances 0.000 abstract description 36
230000006866 deterioration Effects 0.000 abstract description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 5
125000001624 naphthyl group Chemical group 0.000 abstract description 3
150000003624 transition metals Chemical group 0.000 abstract description 3
238000004321 preservation Methods 0.000 abstract 1
229920001577 copolymer Polymers 0.000 description 35
239000010410 layer Substances 0.000 description 29
125000000217 alkyl group Chemical group 0.000 description 19
-1 ogisasol ring Chemical group 0.000 description 18
125000001424 substituent group Chemical group 0.000 description 12
229920002554 vinyl polymer Polymers 0.000 description 8
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 7
125000004432 carbon atom Chemical group C* 0.000 description 7
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
239000010936 titanium Substances 0.000 description 6
229910052719 titanium Inorganic materials 0.000 description 6
229910052782 aluminium Inorganic materials 0.000 description 5
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
239000011248 coating agent Substances 0.000 description 5
238000000576 coating method Methods 0.000 description 5
238000007334 copolymerization reaction Methods 0.000 description 5
150000002334 glycols Chemical class 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
125000004433 nitrogen atom Chemical group N* 0.000 description 5
239000004925 Acrylic resin Substances 0.000 description 4
229920000178 Acrylic resin Polymers 0.000 description 4
239000000020 Nitrocellulose Substances 0.000 description 4
229920002292 Nylon 6 Polymers 0.000 description 4
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 4
150000007513 acids Chemical class 0.000 description 4
125000004453 alkoxycarbonyl group Chemical group 0.000 description 4
GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
125000005843 halogen group Chemical group 0.000 description 4
125000000623 heterocyclic group Chemical group 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
229920001220 nitrocellulos Polymers 0.000 description 4
229920005749 polyurethane resin Polymers 0.000 description 4
239000002904 solvent Substances 0.000 description 4
229920005992 thermoplastic resin Polymers 0.000 description 4
229910052845 zircon Inorganic materials 0.000 description 4
GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
239000005977 Ethylene Substances 0.000 description 3
239000004677 Nylon Substances 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
125000002252 acyl group Chemical group 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
125000003545 alkoxy group Chemical group 0.000 description 3
125000005196 alkyl carbonyloxy group Chemical group 0.000 description 3
125000004429 atom Chemical group 0.000 description 3
239000002585 base Substances 0.000 description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
238000009833 condensation Methods 0.000 description 3
230000005494 condensation Effects 0.000 description 3
239000003431 cross linking reagent Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
239000000463 material Substances 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
239000000203 mixture Substances 0.000 description 3
229920001778 nylon Polymers 0.000 description 3
239000004417 polycarbonate Substances 0.000 description 3
229920000515 polycarbonate Polymers 0.000 description 3
239000004065 semiconductor Substances 0.000 description 3
125000006850 spacer group Chemical group 0.000 description 3
GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
229920002302 Nylon 6,6 Polymers 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
239000004721 Polyphenylene oxide Substances 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
229920000147 Styrene maleic anhydride Polymers 0.000 description 2
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
239000011354 acetal resin Substances 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
150000004703 alkoxides Chemical class 0.000 description 2
125000004390 alkyl sulfonyl group Chemical group 0.000 description 2
125000004414 alkyl thio group Chemical group 0.000 description 2
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
125000003277 amino group Chemical group 0.000 description 2
125000004391 aryl sulfonyl group Chemical group 0.000 description 2
125000004104 aryloxy group Chemical group 0.000 description 2
230000008033 biological extinction Effects 0.000 description 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
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125000004093 cyano group Chemical group *C#N 0.000 description 2
125000000524 functional group Chemical group 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical group 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
239000011976 maleic acid Substances 0.000 description 2
229910052759 nickel Inorganic materials 0.000 description 2
229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 2
229920002401 polyacrylamide Polymers 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
229920000098 polyolefin Polymers 0.000 description 2
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SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
229920003048 styrene butadiene rubber Polymers 0.000 description 2
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 2
150000003505 terpenes Chemical class 0.000 description 2
235000007586 terpenes Nutrition 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
238000005809 transesterification reaction Methods 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
239000008096 xylene Substances 0.000 description 2
WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 1
WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 1
JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 1
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 description 1
IZMZREOTRMMCCB-UHFFFAOYSA-N 1,4-dichloro-2-ethenylbenzene Chemical compound ClC1=CC=C(Cl)C(C=C)=C1 IZMZREOTRMMCCB-UHFFFAOYSA-N 0.000 description 1
125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
UVHXEHGUEKARKZ-UHFFFAOYSA-N 1-ethenylanthracene Chemical compound C1=CC=C2C=C3C(C=C)=CC=CC3=CC2=C1 UVHXEHGUEKARKZ-UHFFFAOYSA-N 0.000 description 1
HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
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JMMZCWZIJXAGKW-UHFFFAOYSA-N 2-methylpent-2-ene Chemical compound CCC=C(C)C JMMZCWZIJXAGKW-UHFFFAOYSA-N 0.000 description 1
KXYAVSFOJVUIHT-UHFFFAOYSA-N 2-vinylnaphthalene Chemical compound C1=CC=CC2=CC(C=C)=CC=C21 KXYAVSFOJVUIHT-UHFFFAOYSA-N 0.000 description 1
PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
FEIQOMCWGDNMHM-UHFFFAOYSA-N 5-phenylpenta-2,4-dienoic acid Chemical compound OC(=O)C=CC=CC1=CC=CC=C1 FEIQOMCWGDNMHM-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
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ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical class N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 description 1
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101001053754 Homo sapiens Type II iodothyronine deiodinase Proteins 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
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JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
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NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
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KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
102100024060 Type II iodothyronine deiodinase Human genes 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
SMEGJBVQLJJKKX-HOTMZDKISA-N [(2R,3S,4S,5R,6R)-5-acetyloxy-3,4,6-trihydroxyoxan-2-yl]methyl acetate Chemical compound CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)O)OC(=O)C)O)O SMEGJBVQLJJKKX-HOTMZDKISA-N 0.000 description 1
FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
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CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthene Chemical compound C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 description 1
238000006359 acetalization reaction Methods 0.000 description 1
229940081735 acetylcellulose Drugs 0.000 description 1
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
229920006322 acrylamide copolymer Polymers 0.000 description 1
125000005396 acrylic acid ester group Chemical group 0.000 description 1
229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
229920001893 acrylonitrile styrene Polymers 0.000 description 1
125000004442 acylamino group Chemical group 0.000 description 1
125000004423 acyloxy group Chemical group 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
239000003513 alkali Substances 0.000 description 1
125000003282 alkyl amino group Chemical group 0.000 description 1
150000001350 alkyl halides Chemical class 0.000 description 1
125000005153 alkyl sulfamoyl group Chemical group 0.000 description 1
125000005422 alkyl sulfonamido group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
150000001414 amino alcohols Chemical class 0.000 description 1
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 1
229930006722 beta-pinene Natural products 0.000 description 1
235000021152 breakfast Nutrition 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
125000002843 carboxylic acid group Chemical group 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
239000000919 ceramic Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000006482 condensation reaction Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000007822 coupling agent Substances 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
150000003997 cyclic ketones Chemical class 0.000 description 1
230000018044 dehydration Effects 0.000 description 1
238000006297 dehydration reaction Methods 0.000 description 1
125000004663 dialkyl amino group Chemical group 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000000428 dust Substances 0.000 description 1
235000013601 eggs Nutrition 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
229920001249 ethyl cellulose Polymers 0.000 description 1
235000019325 ethyl cellulose Nutrition 0.000 description 1
235000019326 ethyl hydroxyethyl cellulose Nutrition 0.000 description 1
229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
XLLIQLLCWZCATF-UHFFFAOYSA-N ethylene glycol monomethyl ether acetate Natural products COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 1
239000005038 ethylene vinyl acetate Substances 0.000 description 1
229920006226 ethylene-acrylic acid Polymers 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
125000002541 furyl group Chemical group 0.000 description 1
LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
239000011521 glass Substances 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
230000020169 heat generation Effects 0.000 description 1
238000005338 heat storage Methods 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
150000002483 hydrogen compounds Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
239000001863 hydroxypropyl cellulose Substances 0.000 description 1
235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
125000001841 imino group Chemical group [H]N=* 0.000 description 1
229920000554 ionomer Polymers 0.000 description 1
XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
210000003127 knee Anatomy 0.000 description 1
239000003446 ligand Substances 0.000 description 1
230000031700 light absorption Effects 0.000 description 1
235000001510 limonene Nutrition 0.000 description 1
229940087305 limonene Drugs 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000155 melt Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 1
125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
125000005397 methacrylic acid ester group Chemical group 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
239000000025 natural resin Substances 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
OTJVAWSLXKXASD-UHFFFAOYSA-N nickel 2-octylphenol Chemical compound [Ni].CCCCCCCCC1=CC=CC=C1O.CCCCCCCCC1=CC=CC=C1O OTJVAWSLXKXASD-UHFFFAOYSA-N 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical group C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229910052697 platinum Inorganic materials 0.000 description 1
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
229920002492 poly(sulfone) Polymers 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920006393 polyether sulfone Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
229920006380 polyphenylene oxide Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920005996 polystyrene-poly(ethylene-butylene)-polystyrene Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229920001289 polyvinyl ether Polymers 0.000 description 1
238000012545 processing Methods 0.000 description 1
239000011241 protective layer Substances 0.000 description 1
125000003226 pyrazolyl group Chemical group 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
125000000168 pyrrolyl group Chemical group 0.000 description 1
125000005493 quinolyl group Chemical group 0.000 description 1
GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
238000012827 research and development Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
238000007142 ring opening reaction Methods 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229920000638 styrene acrylonitrile Polymers 0.000 description 1
125000000547 substituted alkyl group Chemical group 0.000 description 1
FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
125000001174 sulfone group Chemical group 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
VTLHPSMQDDEFRU-UHFFFAOYSA-N tellane Chemical compound [TeH2] VTLHPSMQDDEFRU-UHFFFAOYSA-N 0.000 description 1
229910000059 tellane Inorganic materials 0.000 description 1
229920001897 terpolymer Polymers 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
229920006163 vinyl copolymer Polymers 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
- G11B7/249—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing organometallic compounds
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
- G11B7/246—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes
- G11B7/247—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes methine or polymethine dyes
- G11B7/2472—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes methine or polymethine dyes cyanine

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Thermal Transfer Or Thermal Recording In General (AREA)
Optical Record Carriers And Manufacture Thereof (AREA)

JP58145294A 1983-08-09 1983-08-09 光記録媒体 Granted JPS6036190A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP58145294A JPS6036190A (ja)	1983-08-09	1983-08-09	光記録媒体

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP58145294A JPS6036190A (ja)	1983-08-09	1983-08-09	光記録媒体

Publications (2)

Publication Number	Publication Date
JPS6036190A true JPS6036190A (ja)	1985-02-25
JPH0441066B2 JPH0441066B2 (fr)	1992-07-07

Family

ID=15381811

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP58145294A Granted JPS6036190A (ja)	1983-08-09	1983-08-09	光記録媒体

Country Status (1)

Country	Link
JP (1)	JPS6036190A (fr)

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1997034903A1 (fr) *	1996-03-21	1997-09-25	Sumitomo Seika Chemicals Co., Ltd.	Complexes benzenedithiol-metal substitues
WO2007119672A1 (fr)	2006-04-10	2007-10-25	Fujifilm Corporation	Support d'enregistrement optique, procédé d'enregistrement d'informations visibles et utilisation d'un colorant
WO2008108406A1 (fr)	2007-03-05	2008-09-12	Fujifilm Corporation	Composé pour résine photosensible, solution de résine photosensible, et procédé de gravure utilisant la solution de résine photosensible
WO2008123010A1 (fr)	2007-03-05	2008-10-16	Fujifilm Corporation	Elément électroluminescent, procédé de fabrication de l'élément électroluminescent, élément optique et procédé de fabrication de l'élément optique
EP1998329A2 (fr)	2007-06-01	2008-12-03	Fujifilm Corporation	Support d'enregistrement d'informations optiques et procédé d'enregistrement d'informations
WO2009022442A1 (fr)	2007-08-16	2009-02-19	Fujifilm Corporation	Procédé pour fabriquer un support sur lequel des informations sont enregistrées par un motif de cuvette
WO2009050858A1 (fr)	2007-10-15	2009-04-23	Fujifilm Corporation	Procédé de nettoyage d'une couche de support d'enregistrement de type en mode thermique, procédé de fabrication d'un produit comportant des creux et des saillies, procédé de fabrication d'un élément électroluminescent et procédé de fabrication d'un élément optique
WO2009110046A1 (fr)	2008-03-05	2009-09-11	富士フイルム株式会社	Procédé de traitement d'une pièce de travail ayant une couche photosensible
WO2009113272A1 (fr)	2008-03-10	2009-09-17	富士フイルム株式会社	Procédé de traitement de moule et procédé de fabrication de moule
EP2110814A1 (fr)	2008-04-18	2009-10-21	Fujifilm Corporation	Procédé de fabrication d'une matrice et procédé de fabrication d'un support d'enregistrement d'informations optiques utilisant ensuite une matrice
WO2009130846A1 (fr)	2008-04-22	2009-10-29	富士フイルム株式会社	Procédé d’exposition au laser, procédé de façonnage d’une couche de résine photosensible et procédé de fabrication d’un modèle de moulage
WO2009136624A1 (fr)	2008-05-09	2009-11-12	富士フイルム株式会社	Composition d'absorption d'ultraviolets
WO2010023790A1 (fr)	2008-08-29	2010-03-04	富士フイルム株式会社	Procédé de fabrication d'un corps de formation de motifs et appareil de traitement de faisceau électromagnétique
WO2010023789A1 (fr)	2008-08-29	2010-03-04	富士フイルム株式会社	Elément de formation de motifs et procédé de fabrication associé
WO2010035483A1 (fr)	2008-09-25	2010-04-01	富士フイルム株式会社	Support d’enregistrement d’informations optique, procédé d’enregistrement d’informations, et colorant complexe métallique azoïque
WO2010041470A1 (fr)	2008-10-10	2010-04-15	富士フイルム株式会社	Support d'enregistrement d'informations optique, procédé d'enregistrement d'informations et photosensibilisateur
EP2216680A2 (fr)	2009-02-04	2010-08-11	FUJIFILM Corporation	Particules fines et leur procédé de production
EP2219053A1 (fr)	2009-02-04	2010-08-18	FUJIFILM Corporation	Film réfléchissant les rayons calorifiques, structure réfléchissant les rayons calorifiques et procédé de fabrication correspondant
WO2010093062A1 (fr)	2009-02-13	2010-08-19	Fujifilm Corporation	Dispositif d'électroluminescence organique, et son procédé de production

Citations (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5087649A (fr) *	1973-11-29	1975-07-14
JPS5816888A (ja) *	1981-07-22	1983-01-31	Mitsui Toatsu Chem Inc	半導体レーザ記録フイルム
JPS5856239A (ja) *	1981-09-28	1983-04-02	Tdk Corp	光記録媒体
JPS59185694A (ja) *	1983-04-07	1984-10-22	Tdk Corp	光記録媒体

1983
- 1983-08-09 JP JP58145294A patent/JPS6036190A/ja active Granted

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5087649A (fr) *	1973-11-29	1975-07-14
JPS5816888A (ja) *	1981-07-22	1983-01-31	Mitsui Toatsu Chem Inc	半導体レーザ記録フイルム
JPS5856239A (ja) *	1981-09-28	1983-04-02	Tdk Corp	光記録媒体
JPS59185694A (ja) *	1983-04-07	1984-10-22	Tdk Corp	光記録媒体

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1997034903A1 (fr) *	1996-03-21	1997-09-25	Sumitomo Seika Chemicals Co., Ltd.	Complexes benzenedithiol-metal substitues
US5856520A (en) *	1996-03-21	1999-01-05	Sumitomo Seika Chemicals Co., Ltd.	Substituted benzenedithiol metal complex
WO2007119672A1 (fr)	2006-04-10	2007-10-25	Fujifilm Corporation	Support d'enregistrement optique, procédé d'enregistrement d'informations visibles et utilisation d'un colorant
WO2008108406A1 (fr)	2007-03-05	2008-09-12	Fujifilm Corporation	Composé pour résine photosensible, solution de résine photosensible, et procédé de gravure utilisant la solution de résine photosensible
WO2008123010A1 (fr)	2007-03-05	2008-10-16	Fujifilm Corporation	Elément électroluminescent, procédé de fabrication de l'élément électroluminescent, élément optique et procédé de fabrication de l'élément optique
EP1998329A2 (fr)	2007-06-01	2008-12-03	Fujifilm Corporation	Support d'enregistrement d'informations optiques et procédé d'enregistrement d'informations
WO2009022442A1 (fr)	2007-08-16	2009-02-19	Fujifilm Corporation	Procédé pour fabriquer un support sur lequel des informations sont enregistrées par un motif de cuvette
WO2009050858A1 (fr)	2007-10-15	2009-04-23	Fujifilm Corporation	Procédé de nettoyage d'une couche de support d'enregistrement de type en mode thermique, procédé de fabrication d'un produit comportant des creux et des saillies, procédé de fabrication d'un élément électroluminescent et procédé de fabrication d'un élément optique
WO2009110046A1 (fr)	2008-03-05	2009-09-11	富士フイルム株式会社	Procédé de traitement d'une pièce de travail ayant une couche photosensible
WO2009113272A1 (fr)	2008-03-10	2009-09-17	富士フイルム株式会社	Procédé de traitement de moule et procédé de fabrication de moule
EP2110814A1 (fr)	2008-04-18	2009-10-21	Fujifilm Corporation	Procédé de fabrication d'une matrice et procédé de fabrication d'un support d'enregistrement d'informations optiques utilisant ensuite une matrice
WO2009130846A1 (fr)	2008-04-22	2009-10-29	富士フイルム株式会社	Procédé d’exposition au laser, procédé de façonnage d’une couche de résine photosensible et procédé de fabrication d’un modèle de moulage
WO2009136624A1 (fr)	2008-05-09	2009-11-12	富士フイルム株式会社	Composition d'absorption d'ultraviolets
WO2010023790A1 (fr)	2008-08-29	2010-03-04	富士フイルム株式会社	Procédé de fabrication d'un corps de formation de motifs et appareil de traitement de faisceau électromagnétique
WO2010023789A1 (fr)	2008-08-29	2010-03-04	富士フイルム株式会社	Elément de formation de motifs et procédé de fabrication associé
WO2010035483A1 (fr)	2008-09-25	2010-04-01	富士フイルム株式会社	Support d’enregistrement d’informations optique, procédé d’enregistrement d’informations, et colorant complexe métallique azoïque
WO2010041470A1 (fr)	2008-10-10	2010-04-15	富士フイルム株式会社	Support d'enregistrement d'informations optique, procédé d'enregistrement d'informations et photosensibilisateur
EP2216680A2 (fr)	2009-02-04	2010-08-11	FUJIFILM Corporation	Particules fines et leur procédé de production
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WO2010093062A1 (fr)	2009-02-13	2010-08-19	Fujifilm Corporation	Dispositif d'électroluminescence organique, et son procédé de production

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Publication number	Publication date
JPH0441066B2 (fr)	1992-07-07

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Date	Code	Title	Description
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Publication	Publication Date	Title
JPS6036190A (ja)	1985-02-25	光記録媒体
JPS6044390A (ja)	1985-03-09	光記録媒体
JPS5981194A (ja)	1984-05-10	光記録媒体
JPS5967092A (ja)	1984-04-16	光記録媒体
JPS6044555A (ja)	1985-03-09	光記録媒体
JPS6044389A (ja)	1985-03-09	光記録媒体
JPS6019587A (ja)	1985-01-31	光記録媒体
JPS6018387A (ja)	1985-01-30	光記録媒体
JPH0472712B2 (fr)	1992-11-18
JPS6044554A (ja)	1985-03-09	光記録媒体
JPS5983695A (ja)	1984-05-15	光記録媒体
JPH0441067B2 (fr)	1992-07-07
JPH0441065B2 (fr)	1992-07-07
JPS6035054A (ja)	1985-02-22	光記録媒体
JPS6047069A (ja)	1985-03-14	光記録媒体
JPS5955794A (ja)	1984-03-30	光記録媒体
JPH0440194B2 (fr)	1992-07-02
JPS60234886A (ja)	1985-11-21	光記録媒体
JPS59192595A (ja)	1984-10-31	光記録媒体
JPS60205841A (ja)	1985-10-17	光記録媒体
JPH0342193B2 (fr)	1991-06-26
JPS60204396A (ja)	1985-10-15	光記録媒体
JPS59124897A (ja)	1984-07-19	光記録媒体
JPS59188855A (ja)	1984-10-26	光記録媒体
JPH0521753B2 (fr)	1993-03-25